Evidence map›Paper›PMID 29747815›Full record

ReviewProgress in molecular biology and translational science2018

Gangliosides in Diabetic Wound Healing.

Duncan Hieu M Dam, Amy S Paller

Abstract readReview
In one paragraph

Review in Progress in molecular biology and translational science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
13.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 2 countries.

Duncan Hieu M DamNorthwestern University, Chicago, IL, United States.
Amy S PallerNorthwestern University, Chicago, IL, United States. Electronic address: apaller@northwestern.edu.
Northwestern University · US

Funding

The Role of Keratinocytes as Independent ThermosensorsP30AR057216 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PALLER, AMY S · 2009 to 2018
$6.0M
Post Graduate Program in Cutaneous BiologyT32AR060710 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Amy S Paller · 2012 to 2026
$2.4M
GANGLIOSIDE GENE MODULATION EFFECT ON CELL MOTILITYR01AR044619 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PALLER, AMY SUSAN · 1998 to 2007
$2.4M
Glycosphingolipids Mediate Diabetic Wound Healing ImpairmentR01AR068375 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PALLER, AMY S · 2016 to 2020
$2.1M
siRNA-gold nanoparticle mediated ganglioside depletion for diabetic wound healingR21AR062898 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MIRKIN, CHAD A., PALLER, AMY S · 2012 to 2013
$455k
NIAMS NIH HHS P30 AR057216NIAMS NIH HHS R01 AR044619NIAMS NIH HHS R01 AR068375NIAMS NIH HHS R21 AR062898NIAMS NIH HHS T32 AR060710
6 · The paper itself

Abstract

An organized series of complicated biological and molecular phenomena is required for normal skin wound healing. These processes depend on normal cellular responses to cytokines, growth factors, and other mediators, such as clotting factors, prostaglandins, free radicals, and nitric oxide. In diabetic ulcers, impaired responses to these molecules lead to abnormalities in vascularization, innervation, matrix reconstruction, and reepithelialization of wounds. keratinocyte migration and proliferation on an extracellular matrix is critical in reepithelialization, but the response to growth factors is blunted in diabetes, including the insulin/IGF-1signaling axis. Ganglioside GM3, a sialylated epidermal glycosphingolipid, has been identified as a key mediator of the inhibition of insulin/IGF-1 signaling in response to factors, such as tumor necrosis factor-alpha (TNF-α) and hyperglycemia. Decreased expression of GM3 and the enzyme required for its synthesis, GM3 synthase (GM3S), leads to increased insulin/IGF-1 receptor signaling and accelerated keratinocyte migration, even in the presence of high glucose levels. GM3 depletion in GM3S knockout diabetic mice and diet-induced diabetic mice treated topically with nanoconstruct-mediated GM3S-targeting gene regulation also accelerates wound healing. These recent observations, coupled with evidence that GM3 depletion reverses distal innervation abnormalities in diabetic mice, suggest that GM3-depleting strategies are a promising new approach for human diabetic wounds.

Indexed as

Wound HealingAnimalsDiabetes MellitusGangliosidesHumansWounds and InjuriesGangliosidesdiabetic ulcersgangliosideganglioside depletionkeratinocyte migrationwound healing

Identifiers

PMID29747815
PMCPMC6432781
OpenAlexW2792710415

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.